US6237368B1 - Process for the regulating or controlling the NOx content of exhaust gases given off during the operating of glass melting furnaces with several burners run alternately - Google Patents
Process for the regulating or controlling the NOx content of exhaust gases given off during the operating of glass melting furnaces with several burners run alternately Download PDFInfo
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- US6237368B1 US6237368B1 US09/202,523 US20252399A US6237368B1 US 6237368 B1 US6237368 B1 US 6237368B1 US 20252399 A US20252399 A US 20252399A US 6237368 B1 US6237368 B1 US 6237368B1
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/346—Controlling the process
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/46—Removing components of defined structure
- B01D53/54—Nitrogen compounds
- B01D53/56—Nitrogen oxides
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- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03B—MANUFACTURE, SHAPING, OR SUPPLEMENTARY PROCESSES
- C03B5/00—Melting in furnaces; Furnaces so far as specially adapted for glass manufacture
- C03B5/16—Special features of the melting process; Auxiliary means specially adapted for glass-melting furnaces
- C03B5/235—Heating the glass
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- G—PHYSICS
- G05—CONTROLLING; REGULATING
- G05D—SYSTEMS FOR CONTROLLING OR REGULATING NON-ELECTRIC VARIABLES
- G05D11/00—Control of flow ratio
- G05D11/02—Controlling ratio of two or more flows of fluid or fluent material
- G05D11/13—Controlling ratio of two or more flows of fluid or fluent material characterised by the use of electric means
- G05D11/135—Controlling ratio of two or more flows of fluid or fluent material characterised by the use of electric means by sensing at least one property of the mixture
- G05D11/138—Controlling ratio of two or more flows of fluid or fluent material characterised by the use of electric means by sensing at least one property of the mixture by sensing the concentration of the mixture, e.g. measuring pH value
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S422/00—Chemical apparatus and process disinfecting, deodorizing, preserving, or sterilizing
- Y10S422/90—Decreasing pollution or environmental impact
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S65/00—Glass manufacturing
- Y10S65/13—Computer control
Definitions
- This invention relates to a method of regulating or controlling the content of NO x in exhaust gases produced during the operation of glass-melting furnaces with several burners which are operated in alternation.
- the DE-OS-3615021 describes a method for the selective catalytic reduction of nitrogen oxides from exhaust gases of internal combustion engines by adding ammonia in a reactor.
- the addition of ammonia is effected in dependence on the NO x -concentration in the exhaust gas, and the NO x -concentration is determined indirectly by measuring operating parameters of the internal combustion engine and subsequently calculating the concentration of nitrogen monoxide and nitrogen dioxide in dependence on at least one selected operating parameter on the internal combustion engine in consideration of families of characteristics.
- Glass-melting furnaces mostly are tank furnaces having a plurality of laterally disposed burners which are operated in alternation.
- the actual heating of the glass-melting furnaces is mostly effected by means of long-distance gas, heating oil or natural gas.
- the exhaust gases produced contain nitrogen oxides, due to fuels, high temperatures or additives.
- NO x ⁇ ⁇ set ⁇ ⁇ n NO x ⁇ ⁇ set ⁇ ( 21 - O 2 ⁇ ⁇ act ) ( 21 - 8 )
- the exhaust gas requires some time to flow from the glass-melting furnace to the pure-gas port of the denitrating plant, in which port the pure gas values are measured in general.
- a NO x -content is measured in the denitrating plant which requires a higher amount of NH 3 than this is actually necessary with the real values in the glass-melting furnace.
- a certain time must elapse before a regulation by means of a simple regulator circuit can be performed to react on the individual combustion breaks of the burners in the glass-melting furnaces.
- the object underlying the invention is to provide a method of regulating or controlling the content of NO x in exhaust gases produced during the operation of glass-melting furnaces with several burners which are operated in alternation, where the known standardization of the setpoint NO x set need not be omitted.
- the deviation xd resulting from such comparison is supplied to a regulator, which adapts the amount of NH 3 to be supplied to the denitrating plant as a correcting variable y for regulating the NO x -content as a regulating variable, and where both the beginning of a combustion break FP + and the end of a combustion break FP ⁇ are each supplied as a signal to a binary signal generator, which supplies the signals with a time delay as time-delayed beginning of a combustion break FP z + or as time-delayed end of a combustion break FP z ⁇ to the regulator, which interrupts the regulation upon receipt of the signal FP z + and adjusts the amount of NH 3 to a lower constant fixed value F 1 by means of a control, the content of NO x in the pure gas, NO x ′, detected by the
- combustion break refers to the interruption of the operation of at least one burner.
- the signal for the beginning of a combustion break FP + is immediately generated whenever the burner is switched off.
- the signal for the end of a combustion break FP ⁇ is immediately generated whenever the burner is switched on again.
- the signal for the time-delayed beginning of a combustion break FP z + is generated by the binary signal generator a certain period after the burner has been switched off.
- the signal for the time-delayed end of a combustion break FP z ⁇ is generated by the binary signal generator a certain period after the burner has been switched on again.
- this time delay ⁇ t which in both cases is the same, two definitions are required for technical reasons.
- ⁇ t is the time required by the exhaust gas to flow from the glass-melting furnace to the point where NH 3 is introduced into the denitrating plant.
- the denitrification not only requires a contacting with NH 3 , but also a contacting with an appropriate catalyst, for instance titanium dioxide.
- ⁇ t is the time required by the exhaust gas to flow from the glass-melting furnace to that point in the denitrating plant, where it is for the first time both contacted with NH 3 and with the used catalyst.
- the lower constant fixed value F 1 represents 5 to 20% of the amount of NH 3 introduced directly before the interruption of the regulation.
- values of the content of NO x in the pure gas, NO x ′ are used as starting values, where the memory element can operate in different ways.
- the fixed value F 2 can for instance represent that amount of NH 3 which was necessary for adjusting the last-measured content of NO x in the pure gas. From the last-measured contents of NO x in the pure gas average values can, however, be formed advantageously, from which then the fixed value F 2 can be calculated. It has surprisingly turned out that by means of the inventive method the disadvantages of the known standardization can be eliminated, where it is possible at the same time to relatively quickly react to fluctuating NO x -contents in the glass-melting furnaces, due to the combustion breaks of the individual burners. In the method in accordance with the invention, the admissible limit values of NH 3 in the pure gas are thus not exceeded.
- the constant fixed value F 1 is 6 to 15% of the amount of NH 3 introduced directly before the interruption of the regulation. This is generally not enough for sufficiently converting the still existing content of NO x in the exhaust gases, where at the same time it can advantageously and easily be avoided that the admissible limit values of NH 3 in the pure gas are exceeded.
- the transformation is effected in a memory element through formation of an average, formed from the contents of NO x in the pure gas, NO x ′, which were measured over a period of 5 to 40 min.
- the regulation can be continued with a fixed value F 2 , which is relatively close to the optimum amount of NH 3 to be supplied, when the signal FP z ⁇ is generated by the binary signal generator, i.e. at the time tFP z ⁇ .
- the period is 12 to 18 min. In general, this period is sufficient to mostly obtain a transformed fixed value F 2 , by means of which the regulation can be continued quickly and easily. To a particular advantage, the period is 15 min.
- the exhaust gases are liberated from SO x , HCl, HF and dust prior to the removal of NO x upon leaving the glass-melting furnaces.
- This has a particularly advantageous effect on the execution of the method in accordance with the invention, as disadvantageous influences, due to the noxious substances SO x , HCl, HF and dust, are eliminated.
- the removal of SO x , HCl and HF at 300 to 500° C. can advantageously be effected in a classical or circulating fluidized bed or in an entrained-bed reactor.
- the exhaust gases are for instance contacted with Ca(OH) 2 .
- the exhaust gases are first of all liberated from SO x , HCl and HF and then passed through an electrostatic dust separator.
- the electrostatic dust separators used are electrostatic filters operating dry.
- the electrostatic separator is not contacted with SO x , HCl and HF, which provides for a relatively small maintenance effort.
- the removal of SO x , HCl and HF is effected in a fluidized bed through addition of Ca(OH) 2 .
- This provides for a relatively complete removal of the noxious substances SO x , HCl and HF with a high efficiency.
- FIG. 1 shows the signal flow diagram in accordance with DIN 19226 of the inventive process for regulating or controlling the NO x -content.
- FIG. 2 shows the signal flow diagram in accordance with DIN 19226 of the known regulation of the content of NO x in exhaust gases produced during the operation of glass-melting furnaces with several burners which are operated in alternation.
- FIG. 3 shows by way of example the flow rate of the amount of NH 3 , ⁇ dot over (V) ⁇ NH 3 , to be supplied to the denitrating plant, as a function of the time t in accordance with the inventive method.
- FIG. 1 represents the inventive method of regulating or controlling the content of NO x in exhaust gases.
- the setpoint NO x set predetermined by the setpoint transmitter 1 is supplied to the multiplier 2 .
- the content of O 2 in the pure gas, O 2 act is measured, and the content of O 2 detected in the first transducer 3 , O 2 act′, is likewise supplied to the multiplier 2 .
- the setpoint NO x set is standardized to obtain the standardized setpoint NO x set n in consideration of the content O 2 act′ detected in the first transducer 3 .
- the standardized setpoint NO x set n is compared with the content of NO x in the pure gas, NO x ′, which was detected in the second transducer 6 .
- the resulting deviation xd is supplied to a regulator 4 , which adapts the amount of NH 3 to be supplied to the denitrating plant 5 as a correcting variable y for regulating the NO x -content as a regulating variable.
- the regulator 4 is understood to be the combination of regulator, actuator and controller.
- the signal of the beginning of a combustion break FP + and the signal of the end of a combustion break FP ⁇ is each supplied to a binary signal generator 8 . With a time delay, the binary signal generator 8 supplies the signals FP z + or FP z ⁇ to the regulator 4 .
- the regulation is interrupted by the regulator 4 , and the amount of NH 3 is adjusted to a lower constant fixed value F 1 via a control.
- the content of NO x in the pure gas, NO x ′, which was detected by the second transducer 6 is supplied to a memory element 7 , where it is transformed to a higher constant fixed value F 2 as amount of NH 3 .
- the memory element 7 is advantageously used for the formation of the average, formed from the content of NO x in the pure gas, NO x ′, measured over a period of 5 to 30 min, from which then the associated fixed value F 2 is calculated as amount of NH 3 and supplied to the regulator 4 .
- the regulator 4 As soon as the regulator 4 has received the signal FP z ⁇ , the fixed value F 1 is switched over to the fixed value F 2 via a control. Directly thereafter, the regulation is continued.
- the exhaust gases Prior to the removal of NO x , the exhaust gases can advantageously be liberated from SO x , HCl, HF and dust (not represented), as soon as they have left the glass-melting furnaces.
- FIG. 2 represents the generally known regulation of the content of NO x in exhaust gases produced during the operation of glass-melting furnaces with several burners which are operated in alternation, by means of a simple regulator circuit.
- the known standardization and the slow regulation due to the relatively long distance to be covered by the exhaust gases from the point of introduction of NH 3 to the point where the pure gas is measured in the denitrating plant 5 have a disadvantageous effect in this known regulation.
- FIG. 3 represents by way of example the function of the amount of NH 3 to be supplied to the denitrating plant, ⁇ dot over (V) ⁇ NH 3 , as a function of the time t. 15 min before the time at which the signal FP + is generated, i.e. 15 min before tFP + , the individual measured contents of NO x in the pure gas, NO x ′, are stored in the memory element 7 , the average is formed, and subsequently a fixed value F 2 is defined as amount of NH 3 .
- the advantage is that there is a relatively fast change-over from the fixed value F 1 to the fixed value F 2 at the point tFP z ⁇ , and this change-over is not connected with any regulation-related delay.
- the fixed value F 2 is reached, and proceeding from this fixed value F 2 , which is very close to the optimum value of the amount of NH 3 to be supplied at this time, the regulation may be continued in an advantageous manner.
- the time delay ⁇ t either is the time required by the exhaust gas to flow from the glass-melting furnace to the point of introduction of NH 3 or the time required by the exhaust gas to flow from the glass-melting furnace to that point where the exhaust gas is contacted for the first time with NH 3 and a catalyst, for instance titanium dioxide. This depends on the temperatures of the exhaust gas.
- a catalyst for instance titanium dioxide. This depends on the temperatures of the exhaust gas.
- the 15-minute period is illustrated only by way of example. It may comprise a period of 5 to 40 min, advantageously 12 to 18 min.
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Abstract
A method for regulating or controlling the content of NOx in the exhaust gases of a glass-melting furnace having several burners operated in alternation, wherein both the beginning and the end of a combustion break (FP+, FP−) are supplied to a binary signal generator (8) which passes a signal to a regulator (4) with a time delay and upon receipt of the time-regulator (4), and the amount of NH3 supplied to the denitrating plant is adjusted to a lower constant fixed value F1 via a control, and by means of a memory element (7) a higher constant fixed value F2 is calculated as amount of NH3 and supplied to the regulator (4), whereupon as soon as the regulator (4) has received the signal of the time-delayed end of a combustion break, the fixed value F1 is adjusted to the fixed value F2 via a control, and subsequently the regulation is directly continued.
Description
This invention relates to a method of regulating or controlling the content of NOx in exhaust gases produced during the operation of glass-melting furnaces with several burners which are operated in alternation.
Methods of reducing nitrogen oxides in exhaust gases are known. The DE-OS-3615021 describes a method for the selective catalytic reduction of nitrogen oxides from exhaust gases of internal combustion engines by adding ammonia in a reactor. In accordance with this method the addition of ammonia is effected in dependence on the NOx-concentration in the exhaust gas, and the NOx-concentration is determined indirectly by measuring operating parameters of the internal combustion engine and subsequently calculating the concentration of nitrogen monoxide and nitrogen dioxide in dependence on at least one selected operating parameter on the internal combustion engine in consideration of families of characteristics.
In Römpps Chemie-Lexikon, 8th edition, pp. 1484 to 1490 the operation of glass-melting furnaces is described in detail. Glass-melting furnaces mostly are tank furnaces having a plurality of laterally disposed burners which are operated in alternation. The actual heating of the glass-melting furnaces is mostly effected by means of long-distance gas, heating oil or natural gas. The exhaust gases produced contain nitrogen oxides, due to fuels, high temperatures or additives. During the denitrification of exhaust gases, the NOx-content of the pure gas must, for legal reasons, always be monitored in connection with the O2-content of the pure gas, which leads to the fact that in practice the setpoint of the NOx-content, NOxset, is transformed into a standardized setpoint NOxset n. In general, the following relation is used for the standardization:
However, this standardization is disadvantageous when the glass-melting furnaces comprise several burners which are operated in alternation. If one burner is switched off during a combustion break, the NOx-content of the exhaust gas drops to a relatively large extent. When regulating the content of NOx in the exhaust gases by means of a simple regulator circuit, the introduced amount of NH3, which reacts with the nitrogen oxides in a known manner, is dependent on the deviation xd, wherein:
With decreasing NOx-content of the exhaust gases both the value NOxset n and the value NOx′ are decreased, which leads to the fact that the deviation xd does not or only insignificantly change. Since with a reduction of the content of NOx in the exhaust gases the deviation xd changes only insignificantly, the amount of NH3 to be supplied likewise remains almost constant in the denitrating plant, which leads to the fact that more NH3 is introduced than can be reacted with the nitrogen oxides. This in turn leads to the fact that the content of NH3 in the pure gas generally exceeds the admissible limit values. A further disadvantage of this conventional known regulation lies in the fact that the denitrating plant is generally not arranged in direct vicinity of the glass-melting furnaces. Thus, the exhaust gas requires some time to flow from the glass-melting furnace to the pure-gas port of the denitrating plant, in which port the pure gas values are measured in general. When the operation of a burner is interrupted, a NOx-content is measured in the denitrating plant which requires a higher amount of NH3 than this is actually necessary with the real values in the glass-melting furnace. Thus, a certain time must elapse before a regulation by means of a simple regulator circuit can be performed to react on the individual combustion breaks of the burners in the glass-melting furnaces.
The object underlying the invention is to provide a method of regulating or controlling the content of NOx in exhaust gases produced during the operation of glass-melting furnaces with several burners which are operated in alternation, where the known standardization of the setpoint NOxset need not be omitted. By means of this method a relatively quick reaction to fluctuating NOx-contents during combustion breaks of individual burners in the glass-melting furnace should furthermore be possible.
The object underlying the invention is solved by a method of regulating or controlling the content of NOx in exhaust gases produced during the operation of glass-melting furnaces with several burners which are operated in alternation, where the setpoint of the NOx-content, NOxset, is supplied to a multiplier, at the same time the content of O2 in the pure gas, O2act, is measured continuously, and the content of O2 detected in a first transducer, O2act′, is likewise supplied to the multiplier, and in the multiplier a standardization of the setpoint NOxset into a standardized setpoint NOxset n is effected, where the following applies for the standardization:
and where the standardized setpoint NOxset n is compared with the content of NOx in the pure gas, NOx′, which has been detected by a second transducer, the deviation xd resulting from such comparison is supplied to a regulator, which adapts the amount of NH3 to be supplied to the denitrating plant as a correcting variable y for regulating the NOx-content as a regulating variable, and where both the beginning of a combustion break FP+ and the end of a combustion break FP− are each supplied as a signal to a binary signal generator, which supplies the signals with a time delay as time-delayed beginning of a combustion break FPz + or as time-delayed end of a combustion break FPz − to the regulator, which interrupts the regulation upon receipt of the signal FPz + and adjusts the amount of NH3 to a lower constant fixed value F1 by means of a control, the content of NOx in the pure gas, NOx′, detected by the second transducer is supplied to a memory element, where it is transformed into a higher constant fixed value F2 as amount of NH3, which is likewise supplied to the regulator, and where, as soon as the regulator has received the signal FPz −, the fixed value F1 is adjusted to the fixed value F2 via a control, and directly subsequent thereto the regulation is continued. As glass-melting furnaces there are generally used pot furnaces or tank furnaces, which operate continuously or discontinuously and comprise several burners. The term“burner” not only includes the heatings with long-distance gas, heating oil or natural gas, but also heating electrodes. The term “combustion break” refers to the interruption of the operation of at least one burner. The signal for the beginning of a combustion break FP+ is immediately generated whenever the burner is switched off. The signal for the end of a combustion break FP− is immediately generated whenever the burner is switched on again. The signal for the time-delayed beginning of a combustion break FPz + is generated by the binary signal generator a certain period after the burner has been switched off. The signal for the time-delayed end of a combustion break FPz − is generated by the binary signal generator a certain period after the burner has been switched on again. In the definition of this time delay Δt, which in both cases is the same, two definitions are required for technical reasons. When the temperature of the exhaust gases lies between 750 and 1100° C., the denitrification can be effected by addition of NH3 without a catalyst being present. In this case, Δt is the time required by the exhaust gas to flow from the glass-melting furnace to the point where NH3 is introduced into the denitrating plant. When the temperatures of the exhaust gases lie in the range between 300 and 450° C., the denitrification not only requires a contacting with NH3, but also a contacting with an appropriate catalyst, for instance titanium dioxide. In this case Δt is the time required by the exhaust gas to flow from the glass-melting furnace to that point in the denitrating plant, where it is for the first time both contacted with NH3 and with the used catalyst. The lower constant fixed value F1 represents 5 to 20% of the amount of NH3 introduced directly before the interruption of the regulation. During the transformation of the fixed value F2, values of the content of NOx in the pure gas, NOx′, are used as starting values, where the memory element can operate in different ways. The fixed value F2 can for instance represent that amount of NH3 which was necessary for adjusting the last-measured content of NOx in the pure gas. From the last-measured contents of NOx in the pure gas average values can, however, be formed advantageously, from which then the fixed value F2 can be calculated. It has surprisingly turned out that by means of the inventive method the disadvantages of the known standardization can be eliminated, where it is possible at the same time to relatively quickly react to fluctuating NOx-contents in the glass-melting furnaces, due to the combustion breaks of the individual burners. In the method in accordance with the invention, the admissible limit values of NH3 in the pure gas are thus not exceeded.
In accordance with a preferred aspect of the invention the constant fixed value F1 is 6 to 15% of the amount of NH3 introduced directly before the interruption of the regulation. This is generally not enough for sufficiently converting the still existing content of NOx in the exhaust gases, where at the same time it can advantageously and easily be avoided that the admissible limit values of NH3 in the pure gas are exceeded.
In accordance with a further preferred aspect of the invention the transformation is effected in a memory element through formation of an average, formed from the contents of NOx in the pure gas, NOx′, which were measured over a period of 5 to 40 min. Advantageously, the regulation can be continued with a fixed value F2, which is relatively close to the optimum amount of NH3 to be supplied, when the signal FPz − is generated by the binary signal generator, i.e. at the time tFPz −.
In accordance with a further aspect of the invention the period is 12 to 18 min. In general, this period is sufficient to mostly obtain a transformed fixed value F2, by means of which the regulation can be continued quickly and easily. To a particular advantage, the period is 15 min.
In accordance with a further preferred aspect of the invention, the exhaust gases are liberated from SOx, HCl, HF and dust prior to the removal of NOx upon leaving the glass-melting furnaces. This has a particularly advantageous effect on the execution of the method in accordance with the invention, as disadvantageous influences, due to the noxious substances SOx, HCl, HF and dust, are eliminated. The removal of SOx, HCl and HF at 300 to 500° C. can advantageously be effected in a classical or circulating fluidized bed or in an entrained-bed reactor. For removing SOx, HCl and HF, the exhaust gases are for instance contacted with Ca(OH)2.
In accordance with a further aspect of the invention, the exhaust gases are first of all liberated from SOx, HCl and HF and then passed through an electrostatic dust separator. The electrostatic dust separators used are electrostatic filters operating dry. Advantageously, the electrostatic separator is not contacted with SOx, HCl and HF, which provides for a relatively small maintenance effort.
In accordance with a further aspect of the invention, the removal of SOx, HCl and HF is effected in a fluidized bed through addition of Ca(OH)2. This provides for a relatively complete removal of the noxious substances SOx, HCl and HF with a high efficiency.
The invention will now be explained in detail and by way of example with reference to the drawing (FIGS. 1 to 3).
FIG. 1 shows the signal flow diagram in accordance with DIN 19226 of the inventive process for regulating or controlling the NOx-content.
FIG. 2 shows the signal flow diagram in accordance with DIN 19226 of the known regulation of the content of NOx in exhaust gases produced during the operation of glass-melting furnaces with several burners which are operated in alternation.
FIG. 3 shows by way of example the flow rate of the amount of NH3, {dot over (V)}NH 3 , to be supplied to the denitrating plant, as a function of the time t in accordance with the inventive method.
FIG. 1 represents the inventive method of regulating or controlling the content of NOx in exhaust gases. The setpoint NOxset predetermined by the setpoint transmitter 1 is supplied to the multiplier 2. At the same time, the content of O2 in the pure gas, O2act, is measured, and the content of O2 detected in the first transducer 3, O2act′, is likewise supplied to the multiplier 2. In the multiplier 2 the setpoint NOxset is standardized to obtain the standardized setpoint NOxset n in consideration of the content O2act′ detected in the first transducer 3. The standardized setpoint NOxset n is compared with the content of NOx in the pure gas, NOx′, which was detected in the second transducer 6. The resulting deviation xd is supplied to a regulator 4, which adapts the amount of NH3 to be supplied to the denitrating plant 5 as a correcting variable y for regulating the NOx-content as a regulating variable. The regulator 4 is understood to be the combination of regulator, actuator and controller. The signal of the beginning of a combustion break FP+ and the signal of the end of a combustion break FP− is each supplied to a binary signal generator 8. With a time delay, the binary signal generator 8 supplies the signals FPz + or FPz − to the regulator 4. Upon receipt of the signal FPz + the regulation is interrupted by the regulator 4, and the amount of NH3 is adjusted to a lower constant fixed value F1 via a control. The content of NOx in the pure gas, NOx′, which was detected by the second transducer 6, is supplied to a memory element 7, where it is transformed to a higher constant fixed value F2 as amount of NH3. The memory element 7 is advantageously used for the formation of the average, formed from the content of NOx in the pure gas, NOx′, measured over a period of 5 to 30 min, from which then the associated fixed value F2 is calculated as amount of NH3 and supplied to the regulator 4. As soon as the regulator 4 has received the signal FPz −, the fixed value F1 is switched over to the fixed value F2 via a control. Directly thereafter, the regulation is continued. Prior to the removal of NOx, the exhaust gases can advantageously be liberated from SOx, HCl, HF and dust (not represented), as soon as they have left the glass-melting furnaces.
FIG. 2 represents the generally known regulation of the content of NOx in exhaust gases produced during the operation of glass-melting furnaces with several burners which are operated in alternation, by means of a simple regulator circuit. The known standardization and the slow regulation due to the relatively long distance to be covered by the exhaust gases from the point of introduction of NH3 to the point where the pure gas is measured in the denitrating plant 5 have a disadvantageous effect in this known regulation.
FIG. 3 represents by way of example the function of the amount of NH3 to be supplied to the denitrating plant, {dot over (V)}NH 3 , as a function of the time t. 15 min before the time at which the signal FP+ is generated, i.e. 15 min before tFP+, the individual measured contents of NOx in the pure gas, NOx′, are stored in the memory element 7, the average is formed, and subsequently a fixed value F2 is defined as amount of NH3. After the time delay Δt, at the point tFPz +, at which the signal FPz + is passed on from the binary signal generator 8 to the regulator 4, the regulation is interrupted and the graph of the function abruptly drops to a fixed value F1 and is kept constant. When the signal of the end of a combustion break FP− is generated at the point tFP−, the graph will only rise again from the fixed value F1 to the fixed value F2 upon expiration of the time delay Δt precisely at the point tFPz −, at which the signal FPz − is supplied from the binary signal generator to the regulator 4. The advantage is that there is a relatively fast change-over from the fixed value F1 to the fixed value F2 at the point tFPz −, and this change-over is not connected with any regulation-related delay. Directly at the point tFPz − the fixed value F2 is reached, and proceeding from this fixed value F2, which is very close to the optimum value of the amount of NH3 to be supplied at this time, the regulation may be continued in an advantageous manner. The time delay Δt either is the time required by the exhaust gas to flow from the glass-melting furnace to the point of introduction of NH3 or the time required by the exhaust gas to flow from the glass-melting furnace to that point where the exhaust gas is contacted for the first time with NH3 and a catalyst, for instance titanium dioxide. This depends on the temperatures of the exhaust gas. In FIG. 3 the 15-minute period is illustrated only by way of example. It may comprise a period of 5 to 40 min, advantageously 12 to 18 min.
Claims (7)
1. A method of regulating or controlling the content of NOx in exhaust gases released from a denitrating plant associated with the operation of glass-melting furnaces with several burners which are operated in alternation, wherein the setpoint of the content of NOx, NOxset, is supplied to a multiplier (2), at the same time the content of O2 in the released gas, O2act, is measured continuously, and the content of O2 detected in a first transducer (3), O2act′, is likewise supplied to the multiplier (2), and in the multiplier (2) a standardization of the setpoint NOxset into a standardized setpoint NOxset n is effected, where the following applies for the standardization:
and where the standardized setpoint NOxset n is compared with the content of NOx in the released gas detected by a second transducer (6), NOx′, the deviation xd resulting from this comparison is supplied to a regulator (4), which adapts an amount of NH3 to be supplied to the denitrating plant (5) as a correcting variable y for reacting with and regulating the content of NOx as regulating variable, and where both the beginning of a combustion break FP+ and the end of a combustion break FP− are each supplied as a signal to a binary signal generator (8), which with a time delay supplies the signals as time-delayed beginning of a combustion break FPz + or as time-delayed end of a combustion break FPz − to the regulator (4), which interrupts the regulation upon receipt of the signal FPz + and adjusts the amount of NH3 to a lower constant fixed value F1 via a control, the amount of NOx in the released gas detected by the second transducer (6), NOx′, is supplied to a memory element (7), transformed there into a higher constant fixed value F2 as amount of NH3, and is likewise supplied to the regulator (4), and where, as soon as the regulator (4) has received the signal FPz −, the fixed value F1 is adjusted to the fixed value F2 via a control, whereafter the regulation is continued immediately.
2. The method according to claim 1, wherein the constant fixed value F1 is 6 to 15% of the amount of NH3 introduced immediately before the interruption of the regulation.
3. The method according to claim 1, wherein where the transformation in the memory element (7) is effected through formation of an average, formed from the contents of NOx in the released gas, NOx′, measured over a period of 5 to 40 min.
4. The method according to claim 3, wherein the period comprises 12 to 18 min.
5. The method according to claim 1, wherein the exhaust gases are liberated from SOx, HCl, HF and dust prior to the removal of NOx upon leaving the glass-melting furnaces.
6. The method according to claim 5, wherein the exhaust gases are first liberated from SOx, HCl and HF and are then passed through an electrostatic dust separator.
7. The method according to claim 6, wherein the removal of SOx, HCl and HF is effected in a fluidized bed through addition of Ca(OH)2.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19624619 | 1996-06-20 | ||
DE19624619A DE19624619C1 (en) | 1996-06-20 | 1996-06-20 | Off-gas NOx content regulation method |
PCT/EP1997/002919 WO1997048481A1 (en) | 1996-06-20 | 1997-06-05 | PROCESS FOR REGULATING OR CONTROLLING THE NOx CONTENT OF EXHAUST GASES GIVEN OFF DURING THE OPERATING OF GLASS MELTING FURNACES WITH SEVERAL BURNERS RUN ALTERNATELY |
Publications (1)
Publication Number | Publication Date |
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US6237368B1 true US6237368B1 (en) | 2001-05-29 |
Family
ID=7797484
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US09/202,523 Expired - Fee Related US6237368B1 (en) | 1996-06-20 | 1997-06-05 | Process for the regulating or controlling the NOx content of exhaust gases given off during the operating of glass melting furnaces with several burners run alternately |
Country Status (7)
Country | Link |
---|---|
US (1) | US6237368B1 (en) |
EP (1) | EP0906148B1 (en) |
BR (1) | BR9709863A (en) |
DE (2) | DE19624619C1 (en) |
IN (1) | IN191439B (en) |
TW (1) | TW448134B (en) |
WO (1) | WO1997048481A1 (en) |
Cited By (5)
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US20040241069A1 (en) * | 2002-05-31 | 2004-12-02 | Ri Kokun | Perfluoride processing apparatus |
EP1537904A1 (en) * | 2003-12-04 | 2005-06-08 | Lurgi Energie und Entsorgung GmbH | Process for controlling the dosing of a sorbent |
US20050172677A1 (en) * | 2001-06-27 | 2005-08-11 | Jensen Leif M. | Process and apparatus for making mineral fibres |
US20060113658A1 (en) * | 2004-11-29 | 2006-06-01 | Tzyy-Jang Tseng | Substrate core and method for fabricating the same |
CN108786401A (en) * | 2018-06-07 | 2018-11-13 | 光大环保技术研究院(南京)有限公司 | A kind of PNCR denitrfying agents spray gun control system and PNCR denitrfying agent spray gun control methods |
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- 1997-06-05 WO PCT/EP1997/002919 patent/WO1997048481A1/en active IP Right Grant
- 1997-06-05 US US09/202,523 patent/US6237368B1/en not_active Expired - Fee Related
- 1997-06-05 EP EP97928147A patent/EP0906148B1/en not_active Expired - Lifetime
- 1997-06-05 BR BR9709863A patent/BR9709863A/en unknown
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Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
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US20050172677A1 (en) * | 2001-06-27 | 2005-08-11 | Jensen Leif M. | Process and apparatus for making mineral fibres |
US8176754B2 (en) * | 2001-06-27 | 2012-05-15 | Rockwool International A/S | Process and apparatus for making mineral fibres |
US20040241069A1 (en) * | 2002-05-31 | 2004-12-02 | Ri Kokun | Perfluoride processing apparatus |
US20060245983A1 (en) * | 2002-05-31 | 2006-11-02 | Ri Kokun | Perfluoride processing apparatus |
US7658890B2 (en) | 2002-05-31 | 2010-02-09 | Hitachi, Ltd. | Perfluoride processing apparatus |
US7666365B2 (en) | 2002-05-31 | 2010-02-23 | Hitachi, Ltd. | Perfluoride processing apparatus |
EP1537904A1 (en) * | 2003-12-04 | 2005-06-08 | Lurgi Energie und Entsorgung GmbH | Process for controlling the dosing of a sorbent |
US20060113658A1 (en) * | 2004-11-29 | 2006-06-01 | Tzyy-Jang Tseng | Substrate core and method for fabricating the same |
CN108786401A (en) * | 2018-06-07 | 2018-11-13 | 光大环保技术研究院(南京)有限公司 | A kind of PNCR denitrfying agents spray gun control system and PNCR denitrfying agent spray gun control methods |
Also Published As
Publication number | Publication date |
---|---|
IN191439B (en) | 2003-12-06 |
BR9709863A (en) | 1999-08-10 |
DE19624619C1 (en) | 1997-07-10 |
TW448134B (en) | 2001-08-01 |
WO1997048481A1 (en) | 1997-12-24 |
EP0906148B1 (en) | 2001-05-09 |
EP0906148A1 (en) | 1999-04-07 |
DE59703509D1 (en) | 2001-06-13 |
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